[zeta]-Chain associated protein 70 and CD38 combined predict the time to first treatment in patients with chronic lymphocytic leukemia

BACKGROUND: [zeta]-Chain associated protein (ZAP)-70 has been proposed as a surrogate marker for immunoglobulin heavy-chain variable region (IgVH) mutation in chronic lymphocytic leukemia (CLL), but it is still not clear whether it is an independent prognostic factor. METHODS: The authors evaluated...

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Veröffentlicht in:Cancer 2005-01, Vol.104 (10), p.2124-2132
Hauptverfasser: Del Giudice, Ilaria, Morilla, Alison, Osuji, Nnenna, Matutes, Estella, Morilla, Ricardo, Burford, Anna, Maravelaki, Sonia, Owusu-Ankomah, Kwasi, Swansbury, John, A'Hern, Roger, Brito-Babapulle, Vasantha, Catovsky, Daniel
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Sprache:eng
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Zusammenfassung:BACKGROUND: [zeta]-Chain associated protein (ZAP)-70 has been proposed as a surrogate marker for immunoglobulin heavy-chain variable region (IgVH) mutation in chronic lymphocytic leukemia (CLL), but it is still not clear whether it is an independent prognostic factor. METHODS: The authors evaluated ZAP-70 expression by flow cytometry in 201 untreated patients and correlated ZAP-70 levels with CD38 expression, genetic abnormalities detected by fluorescence in situ hybridization (FISH), and the time from diagnosis to first treatment. RESULTS: Fifty-seven patients (28%) were positive for ZAP-70 ([ge] 20%). Positive ZAP-70 status was associated with advanced disease stage, atypical morphology, CD38-positive status, trisomy 12, del(6q), or no detectable abnormalities; negative ZAP-70 status was correlated with del(13q) as a sole abnormality. The treatment-free interval (TFI) was 17.7 months for ZAP-70- positive patients and 44.6 months for ZAP-70-negative patients (P < 0.001). Multivariate analysis in 117 patients identified advanced stage, CD38 [ge] 7%, and the absence of del(13q) as a sole abnormality as independent factors for short TFI. Excluding FISH, ZAP-70 status acquired independent prognostic value along with CD38 status. The authors proposed a risk model that combines ZAP-70 and CD38 to identify patients who are likely to progress. When both markers were positive, the TFI was 12 months; when both were negative, the median TFI was 54 months; a median TFI of 26 months was observed in patients who had discordant results (P < 0.00001). CONCLUSIONS: The current findings suggested that both ZAP-70 and CD38 should be tested prospectively in all patients with early-stage CLL. Cancer 2005.
ISSN:0008-543X
DOI:10.1002/cncr.21437